Antimicrobial blue light as a biofilm management therapy at the skin‐implant interface in an ex vivo percutaneous osseointegrated implant model

Author:

Ong Jemi12ORCID,Godfrey Rose2,Nazarian Alexa3,Tam Joshua34,Drake Lynn34,Isaacson Brad2567,Pasquina Paul78,Williams Dustin1279

Affiliation:

1. Department of Biomedical Engineering University of Utah Salt Lake City Utah USA

2. Department of Orthopaedics University of Utah Salt Lake City Utah USA

3. Wellman Center for Photomedicine Massachusetts General Hospital Boston Massachusetts USA

4. Department of Dermatology Harvard Medical School Boston Massachusetts USA

5. The Geneva Foundation Tacoma Washington USA

6. Department of Physical Medicine and Rehabilitation, The Musculoskeletal Injury Rehabilitation Research for Operational Readiness (MIRROR) Uniformed Services University Bethesda Maryland USA

7. The Center for Rehabilitation Sciences Research Uniformed Services University Bethesda Maryland USA

8. Department of Rehabilitation Walter Reed National Military Medical Center Bethesda Maryland USA

9. Department of Pathology University of Utah Salt Lake City Utah USA

Abstract

AbstractBiofilm contamination is often present at the skin‐implant interface of transfemoral osseointegrated implants leading to frequent infection, irritation, and discomfort. New biofilm management regimens are needed as the current standard of washing the site with soap and water is inadequate to manage infection rates. We investigated the potential of antimicrobial blue light, which has reduced risk of resistance development and broad antimicrobial mechanisms. Our lab developed an antimicrobial blue light (aBL) device uniquely designed for an ex vivo system based on an established ovine osseointegrated (OI) implant model with Staphylococcus aureus ATCC 6538 biofilms as initial inocula. Samples were irradiated with aBL or washed for three consecutive days after which they were quantified. Colony‐forming unit (CFU) counts were compared with a control group (bacterial inocula without treatment). After 1 day, aBL administered as a single 6 h dose or two 1 h doses spaced 6 h apart both reduced the CFU count by 1.63 log10 ± 0.02 CFU. Over 3 days of treatment, a positive aBL trend was observed with a maximum reduction of ~2.7 log10 CFU following 6 h of treatment, indicating a relation between multiple days of irradiation and greater CFU reductions. aBL was more effective at reducing the biofilm burden at the skin‐implant interface compared with the wash group, demonstrating the potential of aBL as a biofilm management option.

Funder

Uniformed Services University of the Health Sciences

Publisher

Wiley

Subject

Orthopedics and Sports Medicine

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